反应 #336839

ord-ff1c3bf9e38e4142b276aba472c36225

反应方程式

O=C(O)c1nc(C2CC2)nc(Cl)c1Cl
5,6-dichloro-2-cyclopropyl-4-pyrimidinecarboxylic acid
O=C(O)c1nc(C2CC2)nc(Cl)c1Cl
product
O=C(O)c1nc(C2CC2)nc(Cl)c1Cl
5,6-dichloro-2-cyclopropyl-4-pyrimidinecarboxylic acid
N
ammonia
Nc1nc(C2CC2)nc(C(=O)O)c1Cl
title product
Nc1nc(C2CC2)nc(C(=O)O)c1Cl
6-amino-5-chloro-2-cyclopropyl-4-pyrimidinecarboxylic acid

溶剂

反应条件

温度
80°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    浓缩The solution was concentrated at 50° C.
  2. 2
    其他70 torr (9.3 kPa) pressure to about half volume to remove most of the excess ammonia
  3. 3
    温度cooled to 5° C.
  4. 4
    过滤filtered
  5. 5
    其他The isolated solid was dried in a vacuum oven

实验过程

A mixture of 5,6-dichloro-2-cyclopropyl-4-pyrimidinecarboxylic acid (i.e. the product of Step C1 or C2) (5.1 g, 22 mmol), water (30 mL) and aqueous ammonia (28%, 8 g, 130 mmol) was heated at 80° C. for 3 h. The solution was concentrated at 50° C. and 70 torr (9.3 kPa) pressure to about half volume to remove most of the excess ammonia. The resulting slurry was stirred at 20° C., acidified to pH 2 with aqueous hydrochloric acid, cooled to 5° C. and filtered. The isolated solid was dried in a vacuum oven to afford the title product (4.2 g), a compound of the present invention.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07863220B2uspto-grants-2011_01